Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Dhevi N"'
Autor:
Sivapriya Sivagurunathan, Lakshmi Dhevi N Selvan, Aafaque Ahmad Khan, Sowmya Parameswaran, Harsha Bhattacharjee, Krishna Gogoi, Harsha Gowda, T S Keshava Prasad, Akhilesh Pandey, S Ashok Kumar, Pukhraj Rishi, Ekta Rishi, Dhanashree Ratra, Muna Bhende, Narayanan Janakiraman, Jyotirmay Biswas, Subramanian Krishnakumar
Publikováno v:
Indian Journal of Ophthalmology, Vol 69, Iss 3, Pp 647-654 (2021)
Purpose: Age-related macular degeneration (AMD) is one of the leading causes of irreversible central vision loss in the elderly population. The current study aims to find non-invasive prognostic biomarkers in the urine specimens of the AMD patients.
Externí odkaz:
https://doaj.org/article/b6d55ab1c3c84e798cb4a66ff8c3c716
Autor:
Muthusamy, Babylakshmi, Nguyen, Thong T., Bandari, Aravind K., Basheer, Salah, Selvan, Lakshmi Dhevi N., Chandel, Deepshikha, Manoj, Jesna, Gayen, Srimonta, Seshagiri, Somasekar, Chandra Girimaji, Satish, Pandey, Akhilesh
Publikováno v:
In European Journal of Medical Genetics January 2020 63(1)
Autor:
Marimuthu, Arivusudar, Huang, Tai-Chung, Selvan, Lakshmi Dhevi N., Renuse, Santosh, Nirujogi, Raja Sekhar, Kumar, Praveen, Pinto, Sneha M., Rajagopalan, Sudha, Pandey, Akhilesh, Harsha, H.C., Chatterjee, Aditi
Publikováno v:
In EuPA Open Proteomics September 2014 4:10-17
Autor:
Selvan, Lakshmi Dhevi N., Renuse, Santosh, Kaviyil, Jyothi Embekkat, Sharma, Jyoti, Pinto, Sneha M., Yelamanchi, Soujanya D., Puttamallesh, Vinuth N., Ravikumar, Raju, Pandey, Akhilesh, Prasad, T. S. Keshava, Harsha, H.C.
Publikováno v:
In Journal of Proteomics 31 January 2014 97:287-295
Autor:
Arivusudar Marimuthu, Tai-Chung Huang, Lakshmi Dhevi N. Selvan, Santosh Renuse, Raja Sekhar Nirujogi, Praveen Kumar, Sneha M. Pinto, Sudha Rajagopalan, Akhilesh Pandey, H.C. Harsha, Aditi Chatterjee
Publikováno v:
EuPA Open Proteomics, Vol 4, Iss C, Pp 10-17 (2014)
miRNAs regulate gene expression by binding to cognate mRNAs causing mRNA degradation or translational repression. Mass spectrometry-based proteomic analysis is being widely used to identify miRNA targets. The miR-200b miRNA cluster is often overexpre
Externí odkaz:
https://doaj.org/article/00382d4a63f34bd889c2c169c3ba895f
Autor:
Lakshmi Dhevi N. Selvan, Ranjith Kumar, Karthikeyan Sivaraman, Krishnakumar Subramanian, Debashis Sahoo, Sailaja Elchuri
Publikováno v:
Canadian Journal of Biotechnology, Vol 1, Iss Special Issue-Supplement, Pp 248-248 (2017)
Retinoblastoma is the most common primary intraocular tumor in children. It is the first ever cancer to have a genetic basis where inactivation of RB gene in both the alleles would cause the cancer1. Whole genome sequencing, gene expression studies,
Externí odkaz:
https://doaj.org/article/eaff169075bf4ee78da613e1c50c4bc6
Akademický článek
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Autor:
Ajit Zambre, Jagjot Kainth, Subramanian Krishnakumar, Lakshmi Dhevi N. Selvan, Raghuraman Kannan, Anandhi Upendran, Sowmya Parameswaran, Akilandeswari Balachandran, Zahra Afrasiabi
Publikováno v:
RSC Advances. 8:31510-31514
We describe a novel synthetic strategy for conjugating HMGA2 siRNA and the HMGA aptamer to the nucleolin aptamer and nucleolin antibody, respectively. Our studies demonstrate that these conjugates inhibit cell proliferation in retinoblastoma cells.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::367fc10f8b8f583443e8fdbd800573dd
https://doi.org/10.1039/c8ra06026f
https://doi.org/10.1039/c8ra06026f
Autor:
H C Harsha, Kumaran Kandasamy, Prathibha Ranganathan, Sandhya Rani, Subhashri Ramabadran, Sashikanth Gollapudi, Lavanya Balakrishnan, Sutopa B Dwivedi, Deepthi Telikicherla, Lakshmi Dhevi N Selvan, Renu Goel, Suresh Mathivanan, Arivusudar Marimuthu, Manoj Kashyap, Robert F Vizza, Robert J Mayer, James A Decaprio, Sudhir Srivastava, Samir M Hanash, Ralph H Hruban, Akhilesh Pandey
Publikováno v:
PLoS Medicine, Vol 6, Iss 4, p e1000046 (2009)
Externí odkaz:
https://doaj.org/article/35b6e3956ce14e9f9e71c7803656c37f
Autor:
Salah Basheer, Akhilesh Pandey, Satish Chandra Girimaji, Deepshikha Chandel, Somasekar Seshagiri, Babylakshmi Muthusamy, Srimonta Gayen, Lakshmi Dhevi N. Selvan, Thong T. Nguyen, Aravind K. Bandari, Jesna Manoj
Say-Meyer syndrome is a rare and clinically heterogeneous syndrome characterized by trigonocephaly, short stature, developmental delay and hypotelorism. Nine patients with this syndrome have been reported thus far although no causative gene has yet b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::29f833c2e49690ece9e1a0922eb4a73d
https://europepmc.org/articles/PMC6974397/
https://europepmc.org/articles/PMC6974397/
